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Mini TENS Therapy Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182871
510(k) Type
Traditional
Applicant
Shenzhen Jumper Medical Equipment Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
8/1/2019
Days to Decision
293 days
Submission Type
Statement

Mini TENS Therapy Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182871
510(k) Type
Traditional
Applicant
Shenzhen Jumper Medical Equipment Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
8/1/2019
Days to Decision
293 days
Submission Type
Statement